Canonical Allele Identifier: CA337096895
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs28739288
MyVariant Identifiers: chrMT:g.4530G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4530G>C , J01415.2:m.4530G>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.61G>C ENSP00000355046.4:p.Ala21Pro